A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Subcutaneous JKN2401 Injection in Patients With Moderate-to-Severe Chronic Obstructive Pulmonary Disease (COPD)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
888
JKN2401 subcutaneous injection, Q4W
Placebo subcutaneous injection,Q4W
Annualised rate of moderate or severe COPD exacerbations
Time frame: during 52 weeks of treatment
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